Article Text

THU0643 What factors relate to patients contributing longitudinal data using smartphone technology? findings from ra patients participating in arthritispower registry
  1. WB Nowell1,
  2. H Yun2,
  3. J Willig3,
  4. J Beaumont4,
  5. B Johnson3,
  6. S Ginsberg5,
  7. C Wiedmeyer5,
  8. R Crow-Hercher5,
  9. BJ Johnson5,
  10. S Yang3,
  11. JR Curtis3
  1. 1Global Healthy Living Foundation, Upper Nyack
  2. 2University of Alabama at Birmingham School of Public Health
  3. 3University of Alabama at Birmingham, Birmingham
  4. 4Northwestern University Feinberg School of Medicine, Evanston
  5. 5CreakyJoints, Global Healthy Living Foundation, Upper Nyack, United States


Background Data capture of patient reported outcomes (PROs) is gradually shifting from data collection on paper in medical office settings to use of computer or mobile based technologies between doctor visits. Concerns have been raised that patients may have limited interest in contributing data over time or that they may only record new data when there has been a change in their clinical status.

Objectives The objective of this study was to evaluate the patterns and factors associated with longitudinal PRO data capture among participants in the PCORI-funded Patient Powered Research Network for adult rheumatologic conditions, ArthritisPower.

Methods Patients in the registry were asked to voluntarily complete PROs including the RAPID3 and 4 PROMIS instruments plus disease-specific information via a mobile application (App) on their smartphone or computer. We evaluated the average time it took the patient to record each of the instruments and the total number of unique days that patients recorded PROs on the smartphone. Given the newness of the registry (launched late 2015), longitudinal data was defined as contributing at least 2 sets of PROs on unique calendar days. We tested the hypothesis that patients would contribute longitudinal data only when at least one of their scores exceeded a minimally important difference (MID) of any of the 5 PROs examined (generally 2–3 units for PROMIS instruments; 3.6 units for RAPID3). Demographic factors associated with multiple PRO reports were identified using logistic regression among patients who had been enrolled in the registry for at least 3 months.

Results At the time of analysis, ArthritisPower had recruited 2,103 patients, most (approximately 68%) had RA, and 20% provided their Twitter handle. Average (SD) age was 50 (12); 87% were women. The mean assessment time for each of the PROMIS instruments ranged from a low of 16 seconds (Sleep Disturbance) to a high of 105 seconds (RAPID3). The average score for Pain Interference was 64.3 (SD: 6.3), Physical Function 37.5 (6.5), Sleep Disturbance 59.3 (8.4), Fatigue 64.2 (8.4), and RAPID3 15.7 (5.3). Of 1,946 patients who registered the Smartphone App more than 3 months prior to analysis, 20.6% never contributed any PRO information, 53.3% answered once, and 26.1% answered at least twice. Among patients with longitudinal data (≥2 assessments), the mean change score of PROs between pairwise PRO assessments was <1 point for all instruments (Table). Only 23.1% of patients contributing longitudinal data had a change greater than the MID in any of the 5 PRO measures. Patients with RA (OR: 1.54, 95% CI: 1.14–2.06), biologic use (2.12, 1.43–3.15), and those with Twitter accounts (1.40, 1.08–1.82) were more likely to contribute longitudinal PRO data in the absense of regular reminders.

Conclusions Multiple factors were associated with patients contributing longitudinal PRO data. Patients were willing to contribute longitudinal PRO data even in the absence of a change in their health state exceeding any MID. Additional efforts are needed to engage patients to contribute PRO data over time.

Disclosure of Interest None declared

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